HOSPITAL KIT GP 103— 510(k) K922127

Name: FDA 510(k) clearance K922127
Creator: U.S. Food and Drug Administration
Published: 1993-03-29

Unknown

Savoy Medical Supply Co., Inc.

FDA 510(k) clearance K922127 for HOSPITAL KIT GP 103, Unknown on 1993-03-29. Applicant: Savoy Medical Supply Co., Inc.. Device class: 1.

Clearance details

Applicant: Savoy Medical Supply Co., Inc.
Product code: Code MDM
Device class: Class 1
Regulation: 21 CFR 878.4800
Advisory panel: General, Plastic Surgery
Date received: 1992-05-06
Decision date: 1993-03-29
Decision: Unknown
Clearance type: Traditional
Location: Hauppauge, NY, US

Download summary PDF View on FDA.gov ↗

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K922133 — HOSPITAL KIT SV 1051993-06-07
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K923281 — SV 100200 - SINGLE USE ONLY - STERILE HOSPITAL KIT1993-03-26
K922128 — HOSPITAL KIT EP 1041993-03-23
K922126 — HOSPITAL KIT ENT 11251993-01-21

Adverse events under product code MDM

product code MDM

Injury: 247
Malfunction: 1,516
Total: 1,763

Source: openFDA MAUDE database, 2020-01-01 through 2026-04-23. Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →

Data sourced from openFDA. This site is unofficial and independent of the FDA.